Literature DB >> 20223727

The current status and future of multiple myeloma in the clinic.

Sundar Jagannath1, Robert A Kyle, Antonio Palumbo, David S Siegel, Sonia Cunningham, James Berenson.   

Abstract

It is now recognized that all cases of multiple myeloma (MM) are preceded by the premalignant condition of monoclonal gammopathy of undetermined significance (MGUS). Although patients with MGUS are generally asymptomatic and currently managed by "watch and wait," the identification of high-risk patients whose disease will progress more rapidly to smoldering MM (SMM) and MM aids in timely intervention. The immunomodulatory agents thalidomide and lenalidomide and the proteasome inhibitor bortezomib are now routine components of MM therapy in both first-line and relapsed/ refractory settings. These targeted agents are used in various combinations with chemotherapy for the treatment of both transplantation-ineligible and transplantation-eligible patients. More recently, a trend toward evaluation of 3- and 4-drug multiagent combinations before transplantation and prolongation of primary therapy has generated new treatment paradigms. Ultimately, the physician's choice of therapy and treatment strategy requires consideration of regimen-associated toxicities and integration of the patient's risk, comorbid status, and response and tolerability of previous treatment regimens. Particular attention needs to be paid to baseline and/or treatment-emergent peripheral neuropathy, thrombotic risk, changes in renal function, and bone health. Despite recent advances, all patients with MM eventually relapse, and efforts to identify novel synergistic combinations and new agents are ongoing. This review highlights challenges in the clinic and newer approaches under evaluation for the treatment and/or management of patients with MGUS, SMM, and MM.

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Mesh:

Year:  2010        PMID: 20223727     DOI: 10.3816/CLML.2010.n.003

Source DB:  PubMed          Journal:  Clin Lymphoma Myeloma Leuk        ISSN: 2152-2669


  6 in total

Review 1.  Chemotherapy and signaling: How can targeted therapies supercharge cytotoxic agents?

Authors:  Tetyana V Bagnyukova; Ilya G Serebriiskii; Yan Zhou; Elizabeth A Hopper-Borge; Erica A Golemis; Igor Astsaturov
Journal:  Cancer Biol Ther       Date:  2010-11-01       Impact factor: 4.742

2.  Autocrine amplification of immature myeloid cells by IL-6 in multiple myeloma-infiltrated bone marrow.

Authors:  T Matthes; B Manfroi; A Zeller; I Dunand-Sauthier; B Bogen; B Huard
Journal:  Leukemia       Date:  2015-06-19       Impact factor: 11.528

Review 3.  NF-κB as a Therapeutic Target in Inflammatory-Associated Bone Diseases.

Authors:  T-H Lin; J Pajarinen; L Lu; A Nabeshima; L A Cordova; Z Yao; S B Goodman
Journal:  Adv Protein Chem Struct Biol       Date:  2016-12-09       Impact factor: 3.507

4.  Novel phosphatidylinositol 3-kinase inhibitor NVP-BKM120 induces apoptosis in myeloma cells and shows synergistic anti-myeloma activity with dexamethasone.

Authors:  Yuhuan Zheng; Jing Yang; Jianfei Qian; Liang Zhang; Yong Lu; Haiyan Li; Heather Lin; Yongsheng Lan; Zhiqiang Liu; Jin He; Sungyoul Hong; Sheeba Thomas; Jatin Shah; Veera Baladandayuthapani; Larry W Kwak; Qing Yi
Journal:  J Mol Med (Berl)       Date:  2011-12-30       Impact factor: 4.599

5.  Celastrol inhibits proliferation and induces chemosensitization through down-regulation of NF-κB and STAT3 regulated gene products in multiple myeloma cells.

Authors:  Radhamani Kannaiyan; Hui Sin Hay; Peramaiyan Rajendran; Feng Li; Muthu K Shanmugam; Shireen Vali; Taher Abbasi; Shweta Kapoor; Ashish Sharma; Alan Prem Kumar; Wee-Joo Chng; Gautam Sethi
Journal:  Br J Pharmacol       Date:  2011-11       Impact factor: 8.739

6.  Identification of novel myeloma-specific XBP1 peptides able to generate cytotoxic T lymphocytes: a potential therapeutic application in multiple myeloma.

Authors:  J Bae; R Carrasco; A-H Lee; R Prabhala; Y-T Tai; K C Anderson; N C Munshi
Journal:  Leukemia       Date:  2011-06-10       Impact factor: 11.528

  6 in total

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